Ureaplasma Urealyticum Nucleic Acid

Short Description:

This kit is suitable for the qualitative detection of Ureaplasma urealyticum (UU) in male urinary tract and female genital tract secretion samples in vitro.

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Product Detail

Product Tags

Product Name

HWTS-UR002A-Ureaplasma Urealyticum Nucleic Acid Detection Kit(Fluorescence PCR)

Epidemiology

This kit is intended for in vitro detection of Ureaplasma urealyticum (UU) nucleic acid in male urine, male urethral swab, female cervical swab samples.

Channel

FAM	UU nucleic acid
VIC(HEX)	Internal Control

Technical Parameters

Storage	Liquid：≤-18℃ In dark
Shelf-life	12 months
Specimen Type	male urine, male urethral swab, female cervical swab
Ct	≤38
CV	≤5.0%
LoD	50Copies/reaction
Specificity	There is no cross-reactivity with other STD infection pathogens outside the detection range of the kit, such as Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, herpes simplex virus type 1, and herpes simplex virus type
Applicable Instruments	It can match the mainstream fluorescent PCR instruments on the market.Applied Biosystems 7500 Real-Time PCR SystemsQuantStudio® 5 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems LightCycler®480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection System MA-6000 Real-Time Quantitative Thermal Cycler BioRad CFX96 Real-Time PCR System BioRad CFX Opus 96 Real-Time PCR System

Work Flow

Option 1.

Recommended extraction reagent: Macro & Micro-Test Sample Release Reagent(HWTS-3005-8). The extraction should be strictly conducted according to the instructions.

Option 2.

Recommended extraction reagents: Macro & Micro-Test Viral DNA/RNA Kit (HWTS-3017) (which can be used with Macro & Micro-Test Automatic Nucleic Acid Extractor (HWTS-EQ011)) by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. the extraction should be conducted according to the instructions strictly. The recommended elution volume is 80μL.

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Fluorescence Pcr